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Pascal Reynier

Showing results (81-90 of 245) with videos related to

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Human Mutation|September 23, 2014
Improved locus-specific database for OPA1 mutations allows inclusion of advanced clinical dataMarc Ferré, Angélique Caignard, Dan Milea, et al.
Experimental Neurology|September 21, 2010
Mitochondrial dysfunction and pathophysiology of Charcot-Marie-Tooth disease involving GDAP1 mutationsJulien Cassereau, Arnaud Chevrollier, Naïg Gueguen, et al.
Neurogenetics|July 21, 2009
Adenine nucleotide translocase is involved in a mitochondrial coupling defect in MFN2-related Charcot-Marie-Tooth type 2A diseaseVirginie Guillet, Naïg Gueguen, Christophe Verny, et al.
Metabolites|December 23, 2022
A Metabolomic Profile of Seminal Fluid in Extremely Severe Oligozoopermia Suggesting an Epididymal InvolvementOrianne Serri, Magalie Boguenet, Juan Manuel Chao de la Barca, et al.
Journal of Assisted Reproduction and Genetics|November 19, 2013
Are zona pellucida genes involved in recurrent oocyte lysis observed during in vitro fertilization?Marc Ferré, Patrizia Amati-Bonneau, Catherine Morinière, et al.
International Journal of Molecular Sciences|August 12, 2023
Combined Metabolipidomic and Machine Learning Approach in a Rat Model of Stroke Reveals a Deleterious Impact of Brain Injury on Heart MetabolismXavier Dieu, Sophie Tamareille, Aglae Herbreteau, et al.
Annales De Biologie Clinique|March 3, 2017
Pituitary stalk interruption syndrome: a rare and severe cause of pituitary deficiency Laboratory diagnosis of a newborn caseThomas Boueilh, Corentin Bassi, Stéphanie Rouleau, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|February 3, 2011
Bioenergetic defect associated with mKATP channel opening in a mouse model carrying a mitofusin 2 mutationVirginie Guillet, Naïg Gueguen, Romain Cartoni, et al.
Frontiers in Neurology|April 12, 2021
Use of Next-Generation Sequencing for the Molecular Diagnosis of 1,102 Patients With a Autosomal Optic NeuropathyMajida Charif, Céline Bris, David Goudenège, et al.
Biomedicines|June 24, 2022
A Metabolomic Profiling of Intra-Uterine Growth Restriction in Placenta and Cord Blood Points to an Impairment of Lipid and Energetic MetabolismJuan Manuel Chao de la Barca, Floris Chabrun, Tiphaine Lefebvre, et al.
Pageof 25

Showing results (81-90 of 245) with videos related to

Sort By:
Pageof 25
Human Mutation|September 23, 2014
Improved locus-specific database for OPA1 mutations allows inclusion of advanced clinical dataMarc Ferré, Angélique Caignard, Dan Milea, et al.
Experimental Neurology|September 21, 2010
Mitochondrial dysfunction and pathophysiology of Charcot-Marie-Tooth disease involving GDAP1 mutationsJulien Cassereau, Arnaud Chevrollier, Naïg Gueguen, et al.
Neurogenetics|July 21, 2009
Adenine nucleotide translocase is involved in a mitochondrial coupling defect in MFN2-related Charcot-Marie-Tooth type 2A diseaseVirginie Guillet, Naïg Gueguen, Christophe Verny, et al.
Metabolites|December 23, 2022
A Metabolomic Profile of Seminal Fluid in Extremely Severe Oligozoopermia Suggesting an Epididymal InvolvementOrianne Serri, Magalie Boguenet, Juan Manuel Chao de la Barca, et al.
Journal of Assisted Reproduction and Genetics|November 19, 2013
Are zona pellucida genes involved in recurrent oocyte lysis observed during in vitro fertilization?Marc Ferré, Patrizia Amati-Bonneau, Catherine Morinière, et al.
International Journal of Molecular Sciences|August 12, 2023
Combined Metabolipidomic and Machine Learning Approach in a Rat Model of Stroke Reveals a Deleterious Impact of Brain Injury on Heart MetabolismXavier Dieu, Sophie Tamareille, Aglae Herbreteau, et al.
Annales De Biologie Clinique|March 3, 2017
Pituitary stalk interruption syndrome: a rare and severe cause of pituitary deficiency Laboratory diagnosis of a newborn caseThomas Boueilh, Corentin Bassi, Stéphanie Rouleau, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|February 3, 2011
Bioenergetic defect associated with mKATP channel opening in a mouse model carrying a mitofusin 2 mutationVirginie Guillet, Naïg Gueguen, Romain Cartoni, et al.
Frontiers in Neurology|April 12, 2021
Use of Next-Generation Sequencing for the Molecular Diagnosis of 1,102 Patients With a Autosomal Optic NeuropathyMajida Charif, Céline Bris, David Goudenège, et al.
Biomedicines|June 24, 2022
A Metabolomic Profiling of Intra-Uterine Growth Restriction in Placenta and Cord Blood Points to an Impairment of Lipid and Energetic MetabolismJuan Manuel Chao de la Barca, Floris Chabrun, Tiphaine Lefebvre, et al.
Pageof 25